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150 related items for PubMed ID: 32845068

  • 1. Clinical and genetic characteristics of Stargardt disease in a large Western China cohort: Report 1.
    Liu X, Meng X, Yang L, Long Y, Fujinami-Yokokawa Y, Ren J, Kurihara T, Tsubota K, Tsunoda K, Fujinami K, Li S, East Asia Inherited Retinal Disease Society Study Group.
    Am J Med Genet C Semin Med Genet; 2020 Sep; 184(3):694-707. PubMed ID: 32845068
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  • 5. Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease.
    Qu LH, Jin X, Zeng C, Zhou NG, Liu YH, Lin Y.
    Biosci Rep; 2021 Jun 25; 41(6):. PubMed ID: 33988224
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  • 6. Clinical and molecular characteristics of childhood-onset Stargardt disease.
    Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT.
    Ophthalmology; 2015 Feb 25; 122(2):326-34. PubMed ID: 25312043
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  • 7. Variants in the ABCA4 gene in a Brazilian population with Stargardt disease.
    Salles MV, Motta FL, Martin R, Filippelli-Silva R, Dias da Silva E, Varela P, Costa KA, Chiang JP, Pesquero JB, Sallum JF.
    Mol Vis; 2018 Feb 25; 24():546-559. PubMed ID: 30093795
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  • 9. Highly Variable Disease Courses in Siblings with Stargardt Disease.
    Valkenburg D, Runhart EH, Bax NM, Liefers B, Lambertus SL, Sánchez CI, Cremers FPM, Hoyng CB.
    Ophthalmology; 2019 Dec 25; 126(12):1712-1721. PubMed ID: 31522899
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  • 10. CLASSIFYING ABCA4 MUTATION SEVERITY USING AGE-DEPENDENT ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCE-DERIVED TOTAL LESION SIZE.
    Heath Jeffery RC, Thompson JA, Lamey TM, McLaren TL, McAllister IL, Constable IJ, Mackey DA, De Roach JN, Chen FK.
    Retina; 2021 Dec 01; 41(12):2578-2588. PubMed ID: 34125082
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  • 11. Expanding the Mutation Spectrum in ABCA4: Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort.
    Nassisi M, Mohand-Saïd S, Dhaenens CM, Boyard F, Démontant V, Andrieu C, Antonio A, Condroyer C, Foussard M, Méjécase C, Eandi CM, Sahel JA, Zeitz C, Audo I.
    Int J Mol Sci; 2018 Jul 27; 19(8):. PubMed ID: 30060493
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  • 12. Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient Care.
    Daich Varela M, Laich Y, Hashem SA, Mahroo OA, Webster AR, Michaelides M.
    Ophthalmology; 2023 Nov 27; 130(11):1182-1190. PubMed ID: 37331482
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  • 13. Modification of the PROM1 disease phenotype by a mutation in ABCA4.
    Lee W, Paavo M, Zernant J, Stong N, Laurente Z, Bearelly S, Nagasaki T, Tsang SH, Goldstein DB, Allikmets R.
    Ophthalmic Genet; 2019 Aug 27; 40(4):369-375. PubMed ID: 31576780
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  • 16. Analysis of retinal sublayer thicknesses and rates of change in ABCA4-associated Stargardt disease.
    Whitmore SS, Fortenbach CR, Cheng JL, DeLuca AP, Critser DB, Geary EL, Hoffmann JM, Stone EM, Han IC.
    Sci Rep; 2020 Oct 06; 10(1):16576. PubMed ID: 33024232
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  • 18. Antioxidant Saffron and Central Retinal Function in ABCA4-Related Stargardt Macular Dystrophy.
    Piccardi M, Fadda A, Martelli F, Marangoni D, Magli A, Minnella AM, Bertelli M, Di Marco S, Bisti S, Falsini B.
    Nutrients; 2019 Oct 15; 11(10):. PubMed ID: 31618812
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  • 20. Novel Complex ABCA4 Alleles in Brazilian Patients With Stargardt Disease: Genotype-Phenotype Correlation.
    Salles MV, Motta FL, Dias da Silva E, Varela P, Costa KA, Filippelli-Silva R, Martin RP, Chiang JP, Pesquero JB, Sallum JMF.
    Invest Ophthalmol Vis Sci; 2017 Nov 01; 58(13):5723-5730. PubMed ID: 29114839
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